Pain Relief Pm Capsule, Liquid Filled
FDA Label NDC 69452-507

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bionpharma Inc. for the product Pain Relief Pm (NDC 69452-507). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients (in each capsule), purposes, uses, warnings, do not use, ask a doctor before use if, ask a doctor or pharmacist before use if you are, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

†This product is not manufactured or distributed by the owners of Advil® PM LIQUI-GELS®.

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF PRINTED

SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

READ AND KEEP CARTON FOR COMPLETE WARNINGS AND INFORMATION

Manufactured for:

BIONPHARMA

Princeton, NJ 08540

L0001261

R0326

Lot No.:
Exp. Date:

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